💼 Thermo Fisher Scientific Hiring: CRA (Level I, II, Sr CRA) & Clinical Trial Coordinator II
🏢 Company: Thermo Fisher Scientific (PPD Clinical Research Services)📍 Location: Remote / Onsite, India
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences, Nursing
🧪 Experience: 2 – 4+ Years
💰 Salary: Competitive (Industry Standard)
📝 Job Type: Full-Time | Clinical Research | Trial Monitoring | Global Studies
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
📄 Job Overview
Thermo Fisher Scientific, through its PPD® clinical research services, is hiring multiple roles including Clinical Research Associate (CRA I, CRA II, Sr CRA) and Clinical Trial Coordinator II. These positions allow you to contribute to global clinical trials, ensuring quality, compliance, and delivery of life-changing therapies.
🧑⚕️ Role 1: Clinical Research Associate (CRA I, II, Sr CRA)
- ✔ Monitor investigator sites using risk-based monitoring and root cause analysis.
- ✔ Conduct initiation, monitoring, and close-out visits.
- ✔ Verify data accuracy (SDR, SDV, CRF review).
- ✔ Ensure compliance with protocol, ICH-GCP, SOPs, and regulatory standards.
- ✔ Manage essential documents and maintain audit readiness.
💊 Role 2: Clinical Trial Coordinator II
- ✔ Provide administrative and technical support to project teams.
- ✔ Maintain eTMF, Veeva Vault, CTMS & study trackers.
- ✔ Coordinate regulatory document reviews and submissions.
- ✔ Organize and document global project meetings.
- ✔ Support RBM activities and project managers.
🎁 Benefits of Joining Thermo Fisher
- 🌍 Contribute to global clinical trials with real-world impact.
- 📈 Career growth in a leading CRO environment.
- 🤝 Collaborative, diverse, and flexible workplace.
- 💻 Exposure to cutting-edge decentralized trial models.
For more Job 👇👇
📌 Note Before You Apply:
Update your CV to highlight ICH-GCP knowledge, trial monitoring, site management, and eTMF/CTMS experience for higher selection chances.
How to Apply
🟢 Verified Job via Medical Jobs India – hitechplus.in
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